ClinicalTrials.gg
RecruitingNCT07919249TECAR /SISUpdated Nov 9, 2026

TECAR With Chronic Shoulder Impingement Syndrome

An interventional study of TECAR therapy and Passive TECAR therapy in Shoulder Impingement Syndrome, sponsored by May University in Cairo. Recruiting at 1 site in Egypt. Open to participants aged 30 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by May University in Cairo · Not applicable, Interventional, and Treatment

Updated Nov 9, 2026Now RecruitingFirst site in Egypt+5 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
30 Years to 55 Years
Sex
All
01

Study summary

The study aimed to investigate the adjunctive effects of TECAR therapy in combination with conventional exercises compared with placebo TECAR combined with the same exercise program on pain intensity, shoulder function, range of motion, and muscle strength in individuals with subacromial syndrome.

Read the detailed description

Shoulder pain is the third most common musculoskeletal complaint in orthopedic practice. Shoulder pain affects approximately one-third of people in their lifetime. The prevalence of shoulder pain over one month has ranged between 16% and 30% of the population. One of the most common shoulder problems is shoulder impingement syndrome (SIS). Pain arises from shoulder impingement caused by rotator cuff compression and the subacromial bursa. Subacromial Impingement Syndrome is associated with changes in scapular kinematics, muscle activity, and capsular tightness. Restricted range of motion (ROM) and scapular pain are the primary manifestations of subacromial impingement syndrome (SIS); symptoms most commonly occur during limb abduction between 70-120 degrees and during overhead activities. The main therapeutic goals for individuals with SIS are to reduce pain and improve upper limb functional capacity. A cross-sectional study conducted in Egypt reported that the most common type of shoulder pain is shoulder impingement (SIS), accounting for 38.6% of shoulder pathologies TECAR therapy is a specialized form of energy based on a frequency range of 300 KHZ TO 1 MHZ. It uses high-frequency energy to stimulate cellular biological processes and self-regeneration. This therapy enhances natural physiological function and improves metabolism. TECAR therapy works by increasing temperature within deep dermal layers, which can affect the adipocyte membrane and release free fatty acids. This cellular response triggers the activation of macrophages and other inflammatory mediators, contributing to tissue remodeling. Clinically, Tecer therapy is used to manage soft tissue injuries by reducing edema, accelerating remodeling, and supporting the natural inflammatory process. It also aids in decreasing muscle hypertonicity, enhances tissue regeneration across joints and muscles, and relieves muscle and joint pain. Contributing to improving the range of motion and promoting local blood circulation.

Therefore, the present study aims to compare the effect of TECAR versus placebo, both combined with therapeutic exercise, on pain intensity, function, ROM, and muscle strength in patients with Shoulder impingement syndrome (SIS).

Evidence remains limited specifically regarding the use of TECAR therapy for Subacromial Impingement Syndrome (SIS), as previous studies have compared this treatment only with other adjunctive therapies, lacking a distinct control group receiving conventional treatment. The present study addresses this gap.

02

Conditions studied

  • Shoulder Impingement Syndrome
03

In context

Shoulder Impingement Syndrome

320 studies on the registry are indexed under Shoulder Impingement Syndrome; 62 are open to participants now.

This study's planned enrollment of 42 is below the median of 54 across 271 interventional studies indexed under Shoulder Impingement Syndrome.

Browse Shoulder Impingement Syndrome studies →

Lead sponsor

May University in Cairo is the lead sponsor of 3 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

The criteria were revised on the registry on Nov 9, 2026. See what changed

Ages eligible
30 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Referred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months
  • Participants ranged in age from 30 to 55 years old
  • Numerical pain rating scale (NPRS)≥4:
  • Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and pain at the greater tuberosity of the humerus
  • range 18.5- 29. 9 Kg/m².

Exclusion criteria

Exclusion Criteria:

  • Patients who have a full-thickness rotator cuff tear.
  • History of shoulder or rotator cuff surgery or fracture, glenohumeral joint dislocation, rheumatoid arthritis (affected side).
  • Pharmacological medical treatment that may interfere with the measurements; history of injections in the last three months.
  • Patients who received rehabilitation therapy in the last 3 months.
  • Patients who have symptoms of numbness or tingling in the upper extremity.
  • A history of the following: onset of symptoms due to traumatic injury.
  • Patients who have cognitive or psychiatric disorders or pregnancy.
  • Patients who have a positive Drop arm sign.
  • Patients who have cervical radiculopathy.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    TECAR therapy with conventional exercise

    Patients will receive TECAR therapy and conventional exercise for 6 weeks (3 sessions per week), consisting of 2 sessions per week of TECAR therapy and conventional exercises, and one session of conventional exercises only at-home exercises

    Device: TECAR therapy · Other: conventional exercise

  • Sham comparator
    Passive TECAR therapy

    Patients will receive Sham TECAR therapy and conventional exercise for 6 weeks (3 sessions per week), consisting of 2 sessions per week of Sham TECAR therapy and conventional exercises, and one session of conventional exercises only at-home exercises Both groups completed an identical exercise program consisting of stretching, strengthening, and Scapular stabilization

    Device: Passive TECAR therapy · Other: Conventional exercise:

Interventions

  • DeviceTECAR therapy

    TECAR therapy: Received for 8 sessions during the intervention period. Each session consisted of 20 minutes: 10 minutes in capacitive mode at 100 W, followed by 10 minutes in resistive mode at 200 W. The device was operated at a pulsed frequency,

  • DevicePassive TECAR therapy

    sham treatment by TECAR device for 20 min without producing any waves.

  • Otherconventional exercise

    The program included three stretching exercises to address soft tissue restriction. It specifically targeted the upper trapezius, pectoralis minor, and posterior shoulder capsule. Each stretch was held for 30 seconds and repeated three times, with 30 seconds between repetitions Following the stretching exercises, participants completed a progressive strengthening program targeting the rotator cuff muscles and scapular stabilization. Participants performed strengthening exercises using color-coded elastic resistance bands, with 3 sets of 10 repetitions and 1 minute of rest between sets. Rotator cuff strengthening consisted of shoulder flexion, Abduction, External rotation, and Internal Rotation exercises. Scapular stabilization exercises included serratus anterior, middle trapezius, and lower trapezius muscle strengthening)

  • OtherConventional exercise:

    The program included three stretching exercises to address soft tissue restriction. It specifically targeted the upper trapezius, pectoralis minor, and posterior shoulder capsule. Each stretch was held for 30 seconds and repeated three times, with 30 seconds between repetitions Following the stretching exercises, participants completed a progressive strengthening program targeting the rotator cuff muscles and scapular stabilization. Participants performed strengthening exercises using color-coded elastic resistance bands, with 3 sets of 10 repetitions and 1 minute of rest between sets. Rotator cuff strengthening consisted of shoulder flexion, Abduction, External rotation, and Internal Rotation exercises. Scapular stabilization exercises included serratus anterior, middle trapezius, and lower trapezius muscle strengthening)

06

What researchers measure

Primary outcomes

  1. Numerical pain Rating scale:

    The NPRS was used to assess the patient's shoulder pain intensity. Patients rated their current pain level on an 11-point scale from 0 (no pain) to 10 (worst pain imaginable). Ask participants to mark the point on the pain intensity scale

    Time frame: 6 weeks

  2. Shoulder function using the Shoulder Pain and Disability Index Questionnaire (SPADI):

    The SPADI test consists of 13 items divided into two domains: the pain domain (5 items) and the disability domain (8 items). Each item is assigned a value from 0 to 10 on the NRS; the score ranges from 0 (no difficulty) to 10 (unable to perform). All the responses' ratings will be added and divided by the number of questions in that subscale. The total SPADI score will be calculated as the average of the 2 subscales

    Time frame: 6 weeks

Secondary outcomes

  1. Shoulder Range of motion (ROM) by the Clinometer Smartphone Application

    Clinometer application was used to measure shoulder ROM. The patient stands during shoulder flexion and abduction and is supine on the plinth when measuring internal and external rotation; the shoulder is abducted to 90°, the elbow bent to 90 °, and the forearm is in a neutral position.

    Time frame: 6 weeks

  2. Muscle strength: by (Hand-Held Dynamometry)

    Isometric shoulder joint muscle strengths (flexion, abduction, external rotation) were measured with an HHD. The patient performs a maximal isometric muscle contraction for 3 seconds while the hand-held dynamometer is attached. The measurement is repeated three times, with a 30-second rest period between each measurement.

    Time frame: 6 weeks

07

Study locations

1 of 1 sites recruiting
  • outpatient orthopedic clinics of the Faculty of Physical Therapy, Cairo University.
    Cairo, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Nov 9, 2026
Sites
1 site added — first site in Egypt
Show site
  • outpatient orthopedic clinics of the Faculty of Physical Therapy, Cairo University. · Cairo, Egypt
Nov 9, 2026
Start date
Nov 20, 2026→Nov 4, 2026 (actual)
Nov 9, 2026
Eligibility
1 inclusion criterion edited, 4 added; 1 exclusion criterion edited, 7 added, 1 removed
What changed in the criteria
Inclusion criteria
  • AddedReferred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months
  • AddedParticipants ranged in age from 30 to 55 years old
  • AddedNumerical pain rating scale (NPRS)≥4:
  • Edited1. Referred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months 2. Participants ranged in age from 30 to 55 years old 3. Numerical pain rating scale (NPRS)≥4: 4. Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and pain at the greater tuberosity of the humerus 5. BMI range 18.5- 29. 9 Kg/m².
  • AddedBMI range 18.5- 29. 9 Kg/m².
Exclusion criteria
  • AddedPatients who have a full-thickness rotator cuff tear.
  • Edited(1) Patients who have a full-thickness rotator cuff tear. (2) History of shoulder or rotator cuff surgery or fracture, glenohumeral joint dislocation, rheumatoid arthritis (affected side).
  • RemovedPatients who received rehabilitation therapy in the last 3 months. (5) Patients who have symptoms of numbness or tingling in the upper extremity. (6) A history of the following: onset of symptoms due to traumatic injury. (7) Patients who have cognitive or psychiatric disorders or pregnancy. (8) Patients who have a positive Drop arm sign. (9) Patients who have cervical radiculopathy.
  • AddedPatients who received rehabilitation therapy in the last 3 months.
  • AddedPatients who have symptoms of numbness or tingling in the upper extremity.
  • AddedA history of the following: onset of symptoms due to traumatic injury.
  • AddedPatients who have cognitive or psychiatric disorders or pregnancy.
  • AddedPatients who have a positive Drop arm sign.
  • AddedPatients who have cervical radiculopathy.
Nov 9, 2026
Title
TECAR With Shoulder Chronic Shoulder Impingement Syndrome
Nov 9, 2026
Registered
First appeared on the registry
Nov 5, 2026
Show all 2 updates
  1. Nov 9, 2026
    Not yet recruiting→Recruiting
    1 site added — first site in Egypt
    Show site
    • outpatient orthopedic clinics of the Faculty of Physical Therapy, Cairo University. · Cairo, Egypt
    Start date Nov 20, 2026→Nov 4, 2026 (now actual)
    Eligibility 1 inclusion criterion edited, 4 added; 1 exclusion criterion edited, 7 added, 1 removed
    What changed in the criteria
    Inclusion criteria
    • AddedReferred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months
    • AddedParticipants ranged in age from 30 to 55 years old
    • AddedNumerical pain rating scale (NPRS)≥4:
    • Edited1. Referred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months 2. Participants ranged in age from 30 to 55 years old 3. Numerical pain rating scale (NPRS)≥4: 4. Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and pain at the greater tuberosity of the humerus 5. BMI range 18.5- 29. 9 Kg/m².
    • AddedBMI range 18.5- 29. 9 Kg/m².
    Exclusion criteria
    • AddedPatients who have a full-thickness rotator cuff tear.
    • Edited(1) Patients who have a full-thickness rotator cuff tear. (2) History of shoulder or rotator cuff surgery or fracture, glenohumeral joint dislocation, rheumatoid arthritis (affected side).
    • RemovedPatients who received rehabilitation therapy in the last 3 months. (5) Patients who have symptoms of numbness or tingling in the upper extremity. (6) A history of the following: onset of symptoms due to traumatic injury. (7) Patients who have cognitive or psychiatric disorders or pregnancy. (8) Patients who have a positive Drop arm sign. (9) Patients who have cervical radiculopathy.
    • AddedPatients who received rehabilitation therapy in the last 3 months.
    • AddedPatients who have symptoms of numbness or tingling in the upper extremity.
    • AddedA history of the following: onset of symptoms due to traumatic injury.
    • AddedPatients who have cognitive or psychiatric disorders or pregnancy.
    • AddedPatients who have a positive Drop arm sign.
    • AddedPatients who have cervical radiculopathy.
    Title TECAR With Shoulder Chronic Shoulder Impingement Syndrome
    + 1 other change: contact details
  2. Nov 5, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07919249
Lead sponsor
May University in Cairo
Collaborators
Cairo University
Responsible party
Amgad Tamer Farhat Elkhyat (Dr, May University in Cairo) — Principal investigator
First posted
Nov 5, 2026
Start date
Nov 4, 2026
Primary completion
Dec 20, 2027 (estimated)
Completion
Mar 20, 2028 (estimated)
Last update
Nov 9, 2026

Study contacts

Amgad Tamer Farhat Elkhyat
Contact
amgad.23110702@muc.edu.eg
01090005697
Afaf Mohamed Omar Tahoon, Lecturer
Contact
afaf_tahoon@cu.edu.eg
01015401783
Salma Osama Abdelhameed Eid, Demonstrator
study chair · salma.Eid@bue.edu.eg
Maram Ibrahim Ali Ibrahim, Demonstrator
study chair · Maram.Ibrahim@bue.edu.eg
Tasbih Emad saber
study chair · tasbihemad87@gmail.com
Sama Sayed Mohamed Sayed
study chair · samaasayed268@gmail.com
Alaa Elsayed Atia Hassan
study chair · 10712023100273@stud.cu.edu.eg
Esraa Mohamed Mosaid
study chair · esramohamedmosaid@gmail.com

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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